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128422-75-3

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128422-75-3 Usage

General Description

4-Hydroxyphenyl 4-allyloxybenzoate, also known as "allyl 4-hydroxyphenyl ether benzoate," is a chemical compound with the molecular formula C16H14O4. It is an ester compound consisting of a hydroxyphenyl group and an allyloxybenzoate group. This chemical is often used as an additive in various industrial and consumer products, particularly in cosmetics and personal care products. It is known for its ability to provide UV protection and act as a stabilizer in sunscreens, lotions, and other skincare products. Additionally, it may also be used as a fragrance ingredient and flavoring agent in certain products. Overall, 4-Hydroxyphenyl 4-allyloxybenzoate is valued for its versatile properties and applications in the formulation of various everyday products.

Check Digit Verification of cas no

The CAS Registry Mumber 128422-75-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,8,4,2 and 2 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 128422-75:
(8*1)+(7*2)+(6*8)+(5*4)+(4*2)+(3*2)+(2*7)+(1*5)=123
123 % 10 = 3
So 128422-75-3 is a valid CAS Registry Number.
InChI:InChI=1/C16H14O4/c1-2-11-19-14-7-3-12(4-8-14)16(18)20-15-9-5-13(17)6-10-15/h2-10,17H,1,11H2

128422-75-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (4-hydroxyphenyl) 4-prop-2-enoxybenzoate

1.2 Other means of identification

Product number -
Other names 4-hydroxyphenyl 4'-allyloxybenzoate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:128422-75-3 SDS

128422-75-3Relevant articles and documents

New liquid-crystalline elastomers: 1. Synthesis, structure, and phase behavior of a series of mesogenic crosslinking agents containing reactive bifunctional groups

Xu, Xiao-Xu,Hong, Zhe,Liu, Fei

scheme or table, p. 52 - 62 (2011/09/15)

The synthesis of eight mesogenic crosslinking agents (1c-8c) containing reactive bifunctional groups is described. The chemical structures were characterized by Fourier transform infrared (FTIR) and 1H nuclear magnetic resonance (NMR) spectra. The mesomorphism was investigated by differential scanning calorimetry (DSC) and polarizing optical microscopy (POM). The compounds 1c, 2c, 3c, 5c, 6c, and 8c showed an enantiotropic nematic phase. In addition, 5c exhibited a smectic A (SmA) phase on cooling; 4c exhibited a smectic C (SmC) phase, a SmA phase, and a nematic phase and a monotropic a smectic B (SmB) phase on cooling. 7c revealed an SmA phase and a nematic phase and a monotropic SmC phase on cooling. Copyright Taylor & Francis Group, LLC.

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